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1.
Biofouling ; 39(1): 64-79, 2023 01.
Artigo em Inglês | MEDLINE | ID: mdl-36924139

RESUMO

Biofouling is a major challenge for sustainable shipping, filter membranes, heat exchangers, and medical devices. The development of fouling-resistant coatings requires the evaluation of their effectiveness. Such an evaluation is usually based on the assessment of fouling progression after different exposure times to the target medium (e.g. salt water). The manual assessment of macrofouling requires expert knowledge about local fouling communities due to high variances in phenotypical appearance, has single-image sampling inaccuracies for certain species, and lacks spatial information. Here an approach for automatic image-based macrofouling analysis was presented. A dataset with dense labels prepared from field panel images was made and a convolutional network (adapted U-Net) for the semantic segmentation of different macrofouling classes was proposed. The establishment of macrofouling localization allows for the generation of a successional model which enables the determination of direct surface attachment and in-depth epibiotic studies.


Assuntos
Biofilmes , Incrustação Biológica , Semântica , Incrustação Biológica/prevenção & controle , Processamento de Imagem Assistida por Computador/métodos , Navios
2.
Biofouling ; 38(9): 940-951, 2022 10.
Artigo em Inglês | MEDLINE | ID: mdl-36511186

RESUMO

Biofouling on surfaces in contact with sea- or brackish water can severely impact the function of devices like reverse osmosis modules. Single species laboratory assays are frequently used to test new low fouling materials. The choice of bacterial strain is guided by the natural population present in the application of interest and decides on the predictive power of the results. In this work, the analysis of the bacterial community present in brackish water from Mashabei Sadeh, Israel was performed and Rheinheimera sp. was detected as a prominent microorganism. A Rheinheimera strain was selected to establish a short-term accumulation assay to probe initial bacterial attachment as well as biofilm growth to determine the biofilm-inhibiting properties of coatings. Both assays were applied to model coatings, and technically relevant polymers including laser-induced graphene. This strategy might be applied to other water sources to better predict the fouling propensity of new coatings.


Assuntos
Incrustação Biológica , Polímeros , Biofilmes , Carbono , Propriedades de Superfície , Incrustação Biológica/prevenção & controle , Bactérias , Águas Salinas
3.
ACS Appl Mater Interfaces ; 13(5): 6659-6669, 2021 Feb 10.
Artigo em Inglês | MEDLINE | ID: mdl-33497184

RESUMO

Dendritic polyglycerol (PG) was covalently coupled to 2-hydroxyethyl methacrylate (HEMA) by an anionically catalyzed ring-opening polymerization generating a dendritic PG-HEMA with four PG repetition units (PG4MA). Coatings of the methacrylate monomer were prepared by grafting-through and compared against commercially available hydrophilic monomers of HEMA, poly(ethylene) glycol methacrylate (PEGMA), and poly(propylene) glycol methacrylate (PPGMA). The obtained coatings were characterized by modern surface analytical techniques, including water contact angle goniometry (sessile and captive bubble), attenuated total internal reflection Fourier transform infrared spectroscopy, and atomic force microscopy. The antifouling (AF) and fouling-release (FR) properties of the coatings were tested against the model organisms Cobetia marina and Navicula perminuta in laboratory-scale dynamic accumulation assays as well as in a dynamic short-term field exposure (DSFE) in the marine environment. In addition, the hydration of the coatings and their susceptibility toward silt uptake were evaluated, revealing a strong correlation between water uptake, silt incorporation, and field assay performance. While all glycol derivatives showed good resistance in laboratory settlement experiments, PPGMA turned out to be less susceptible to silt incorporation and outperformed PEGMA and PG4MA in the DSFE assay.


Assuntos
Antibacterianos/farmacologia , Incrustação Biológica/prevenção & controle , Diatomáceas/efeitos dos fármacos , Halomonadaceae/efeitos dos fármacos , Metacrilatos/farmacologia , Antibacterianos/síntese química , Antibacterianos/química , Metacrilatos/síntese química , Metacrilatos/química , Testes de Sensibilidade Microbiana , Estrutura Molecular , Tamanho da Partícula , Propriedades de Superfície , Água/química
4.
ACS Appl Bio Mater ; 4(5): 4191-4200, 2021 05 17.
Artigo em Inglês | MEDLINE | ID: mdl-35006832

RESUMO

Membrane separation processes including reverse osmosis are now considered essential techniques for water and wastewater treatment, especially in water-scarce areas where desalination and water reuse can augment the water supply. However, biofouling remains a significant challenge for these processes and in general for marine biological fouling, which results in increased energy consumption and high operational costs. Especially in flat sheet membrane modules, intense biofilm growth occurs on the feed spacer at points of contact to the membrane surface. Here, we developed an ultrastable superhydrophobic antibiofouling feed spacer that resists biofilm growth. A commercial polypropylene feed spacer was coated with poly(dimethylsiloxane) (PDMS), and then, candle soot nanoparticles (CSNPs) were embedded into the ultrathin layer of PDMS, which resulted in a superhydrophobic nanostructured surface with a contact angle >150°. The CSNP-coated spacer was examined for inhibition of biofilm growth by a cross-flow membrane channel using Pseudomonas aeruginosa (PA01), and the coating was examined for effectiveness in marine fouling by testing the adhesion of marine bacterium Cobetia marina and diatom Navicula perminuta in a dynamic accumulation assay. In all cases, the CSNP coatings showed almost complete elimination of biofilm growth under the conditions tested. Confocal laser scanning microscopy and scanning electron microscopy indicated a 99% reduction in biofilm growth on the modified spacers compared to the uncoated controls. This effect was attributed to the superhydrophobic nanostructured surface, where trapped gasses formed a plastron on the coating. This plastron was observed to be extremely stable over time and could even be replenished at elevated temperatures. Development of similar antibiofouling coatings on feed spacers or other marine applications might lead to improvements in many industrial processes including membrane filtration where increased membrane life span and reduced energy consumption are key to implementation.


Assuntos
Materiais Revestidos Biocompatíveis/química , Dimetilpolisiloxanos/química , Purificação da Água , Água/química , Interações Hidrofóbicas e Hidrofílicas , Teste de Materiais , Nanopartículas/química , Tamanho da Partícula
5.
J Am Chem Soc ; 141(11): 4660-4669, 2019 03 20.
Artigo em Inglês | MEDLINE | ID: mdl-30740972

RESUMO

In cells, proteins are embedded in a crowded environment that controls their properties via manifold avenues including weak protein-macromolecule interactions. A molecular level understanding of these quinary interactions and their contribution to protein stability, function, and localization in the cell is central to modern structural biology. Using a mutational analysis to quantify the energetic contributions of single amino acids to the stability of the ALS related protein superoxide dismutase I (SOD1) in mammalian cells, we show that quinary interactions destabilize SOD1 by a similar energetic offset for most of the mutants, but there are notable exceptions: Mutants that alter its surface properties can even lead to a stabilization of the protein in the cell as compared to the test tube. In conclusion, quinary interactions can amplify and even reverse the mutational response of proteins, being a key aspect in pathogenic protein misfolding and aggregation.


Assuntos
Simulação de Dinâmica Molecular , Mutação Puntual , Superóxido Dismutase-1/genética , Superóxido Dismutase-1/metabolismo , Estabilidade Enzimática , Células HeLa , Humanos , Ligação Proteica , Conformação Proteica , Superóxido Dismutase-1/química
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